Enrolling now · NCT06672939

A study testing whether a GLP-1 medicine from Lilly, orforglipron, can help with weight.

Who can join
Children and teens 12 to 17, have obesity.
What you take
orforglipron, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
How long it lasts
The full study runs about 6.2 years; your own time in it is usually shorter.
What you get
The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
Phase Phase 3Sponsor Eli Lilly and CompanyDrug orforglipronClass GLP-1 RASites 14 USEnrollment target 150

What this study is for

Full study title: A Study of Orforglipron (LY3502970) in Adolescent Participants With Obesity, or Overweight With Related Comorbidities.

Primary condition: Obesity. Also studied in: Overweight.

Who can join, in detail

Age 12 to 17
Sex All

Key inclusion criteria

  • Have a history of at least 1 unsuccessful effort to lose sufficient body weight after participation in a structured lifestyle modification program (diet and exercise counseling for at least 3 months) prior to screening.
  • Obesity as defined by BMI equal to or above the 95th percentile for age and sex (on age- and gender-specific growth chart [CDC-NCHS, 2022]); OR
  • Overweight as defined by BMI equal to or above the 85th percentile but less than the 95th percentile for age and sex, on age- and sex-specific growth chart (CDC-NCHS, 2022), and at least 1 weight-related comorbidity,
  • hypertension
  • type 2 diabetes (T2D)

Key exclusion criteria

  • Prepubertal (Tanner stage 1)
  • Have a self-reported, or by parent or legal guardian where applicable, decrease in body weight greater than 5 kilograms (kg) (11 pounds) within 90 days before screening
  • Have undergone or plan to undergo weight reduction procedure during the study, such as, but not limited to:
  • gastric bypass
  • sleeve gastrectomy

Where this study is enrolling

This trial has 14 US sites across 12 states. Contact the site coordinator directly to start the screening process.

California

  • Carey Chronis MD Pediatric, Infant and Adolescent Medicine
    Ventura, California
    805-642-4704

Connecticut

  • Stamford Therapeutics Consortium
    Stamford, Connecticut
    727-544-4842

Georgia

  • Children's Healthcare of Atlanta - Center for Advanced Pediatrics
    Atlanta, Georgia
    404-712-4731

Illinois

  • Ann & Robert H. Lurie Children's Hospital of Chicago
    Chicago, Illinois
    312-503-1499

Louisiana

  • Velocity Clinical Research
    Lafayette, Louisiana
    337-519-4742

Mississippi

  • MedPharmics, LLC
    Gulfport, Mississippi
    228-206-1283

Missouri

  • Sundance Clinical Research
    St Louis, Missouri
    314-567-3377

North Carolina

  • Lucas Research, Inc.
    Morehead City, North Carolina
    252-222-5700

Pennsylvania

  • Childrens Hospital of Pittsburgh
    Pittsburgh, Pennsylvania
    412-692-6935

Tennessee

  • Vanderbilt Health One Hundred Oaks
    Nashville, Tennessee
    615-322-6000

Texas

  • Dynamed Clinical Research, LP d/b/a DM Clinical Research
    Houston, Texas
  • La Providence Pediatrics Clinic - Chemidox Clinical Trials
    Houston, Texas
    833-324-3643
  • Martin Diagnostic Clinic
    Tomball, Texas

Utah

  • Velocity Clinical Research, Salt Lake City
    South Jordan, Utah

Timeline

Started enrolling: 2024-11-18. Expected completion: 2031-01. Last updated on ClinicalTrials.gov: 2026-05-27.

Official source

We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:

View on ClinicalTrials.gov →

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